An urge to move with L-thyroxine: Clinical, biochemical and, polysomnographic correlation

由 Tan E.-K., Ho S.-C., Koh L., Pavanni R.
出版 2018

Genetic analysis of SCA 2 and 3 repeat expansions in essential tremor and atypical Parkinsonism

由 Tan E.-K., Tong J., Pavanni R., Wong M.-C., Zhao Y.
出版 2018

Case control polysomnographic studies of sleep disorders in Parkinson's disease

由 Yong M.-H., Fook-Chong S., Pavanni R., Lim L.-L., Tan E.-K.
出版 2018

Prescribing pattern in Parkinson's disease: Are cost and efficacy overriding factors?

由 Tan E.-K., Yeo A.P., Tan V., Pavanni R., Wong M.C.
出版 2018

Complementary therapies in hemifacial spasm and comparison with other movement disorders

由 Peeraully T., Hameed S., Cheong P.T., Pavanni R., Hussein K., Fook-Chong S.M.C., Tan E.-K.
出版 2018

Glucocerebrosidase mutations and risk of Parkinson disease in Chinese patients [2]

由 Tan E.-K., Tong J., Fook-Chong S., Yih Y., Wong M.-C., Pavanni R., Zhao Y.
出版 2018

Complementary therapies in hemifacial spasm and comparison with other movement disorders

由 Peeraully, T., Hameed, S., Cheong, P.T., Pavanni, R., Hussein, K., Fook-Chong, S.M.C., Tan, E.-K.
出版 2014

Differential effect of caffeine intake in subjects with genetic susceptibility to Parkinson's Disease

由 Kumar P.M., Paing S.S.T., Li H., Pavanni R., Yuen Y., Zhao Y., Tan E.K.
出版 2018

Analysis of 14 LRRK2 mutations in Parkinson's plus syndromes and late-onset Parkinson's disease

由 Tan E.-K., Skipper L., Chua E., Wong M.-C., Pavanni R., Bonnard C., Kolatkar P., Liu J.-J.
出版 2018

DRD3 variant and risk of essential tremor

由 Tan E.-K., Prakash K.M., Fook-Chong S., Yih Y., Chua E., Lum S.Y., Wong M.C., Pavanni R., Zhao Y.
出版 2018

Case-control study of UCHL1 S18Y variant in Parkinson's disease

由 Tan E.-K., Puong K.-Y., Fook-Chong S., Chua E., Shen H., Yuen Y., Pavanni R., Wong M.-C., Puvan K., Zhao Y.
出版 2018

Analysis of LRRK2 Gly2385Arg genetic variant in non-Chinese Asians

由 Tan E.-K., Zhao Y., Tan L., Lim H.-Q., Lee J., Yuen Y., Pavanni R., Wong M.-C., Fook-Chong S., Liu J.-J.
出版 2018

Genetic analysis of DJ-1 in a cohort Parkinson's disease patients of different ethnicity

由 Tan E.-K., Tan C., Zhao Y., Yew K., Shen H., Chandran V.R., Teoh M.-L., Yih Y., Pavanni R., Wong M.-C.
出版 2018

LRRK2 R1628P increases risk of Parkinson's disease: Replication evidence

由 Tan, E.K., Tan, L.C., Lim, H.Q., Li, R., Tang, M., Yih, Y., Pavanni, R., Prakash, K.M., Fook-Chong, S., Zhao, Y.
出版 2014

Genetic analysis of Nurr1 haplotypes in Parkinson's disease

由 Tan E.-K., Chung H., Zhao Y., Shen H., Chandran V.R., Tan C., Teoh M.-L., Yih Y., Pavanni R., Wong M.-C.
出版 2018

Comprehensive evaluation of common genetic variation within LRRK2 reveals evidence for association with sporadic Parkinson's disease

由 Skipper L., Li Y., Bonnard C., Pavanni R., Yih Y., Chua E., Sung W.-K., Tan L., Wong M.-C., Tan E.-K., Liu J.
出版 2018

Mitochondrial complex I polymorphism and cigarette smoking in Parkinson's disease

由 Tan E.K., Chai A., Zhao Y., Lum S.Y., Fook-Chong S.M.C., Teoh M.L., Yih Y., Pavanni R., Wong M.C.
出版 2018

Nurr1 mutational screen in Parkinson's disease

由 Tan E.-K., Chung H., Chandran V.R., Tan C., Shen H., Yew K., Pavanni R., Puvan K.-A., Wong M.-C., Teoh M.-L., Yih Y., Zhao Y.
出版 2018

Analysis of GWAS-linked loci in Parkinson disease reaffirms PARK16 as a susceptibility locus

由 Tan, E.-K., Kwok, H.-K., Tan, L.C., Zhao, W.-T., Prakash, K.M., Au, W.-L., Pavanni, R., Ng, Y.-Y., Satake, W., Zhao, Y., Toda, T., Liu, J.-J.
出版 2014

Expanded FMR1 alleles are rare in idiopathic Parkinson's disease [3]

由 Tan E.K., Zhao Y., Puong K.Y., Law H.Y., Chan L.L., Yew K., Shen H., Chandran V.R., Yuen Y., Pavanni R., Wong M.C., Ng I.S.
出版 2018